Antiseptic Hand Sanitizer Wipe Benzalkonium Chloride
FDA Label NDC 81063-000
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Canopus Wet Wipes Private Limited for the product Antiseptic Hand Sanitizer Wipe Benzalkonium Chloride (NDC 81063-000). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredient, purpose, use, warnings, do not use, stop use and ask a doctor if:, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.1%
Purpose
Antiseptic
Use
For hand washing to decrease bacteria on ths skin
Warnings
For external use only.
Do Not Use
in the eyes.
Stop Use And Ask A Doctor If:
irritation and redness develop. If condition persists for more than 72 hours consult a doctor.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact poison Control Centre right away.
Directions
Wet hands thoroughly with product and allow to dry without wiping.
Inactive Ingredients
Polyaminopropyl Biguanide, Aloe Barbadensis Extract, Glycerin, Citric acid, EDTA 2Na, Water
Package Labeling:
Label (Label)
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